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About the journal
Journal of Human Genetics is a journal published by Springer Nature in Japan. It is listed in MEDLINE and PUBMED according to the sources read. Declared publication charge: 5,290 EUR. Facts are reproduced as recorded at their sources with their capture dates; PublishLens indicators are available after sign-in.
Basic facts
- Publisher
- Springer Nature
- ISSN
- 1434-5161 · 1435-232X
- Country
- Japan
- Access
- Not open access / not declared
- Declared publication charge
- 5,290 EUR
- Declared peer-review model
- peer_review
- Official website
- http://www.nature.com/jhg/archive/index.html
Index listings
- MEDLINE · 1998-01-01
- PUBMED · 2011-06-16
- Indexing
- MEDLINE · PUBMED
- APC
- 5,290 EUR
- Declared review time (DOAJ)
- —
- Actual review time (measured)
- 107 days received→accepted — computed from PubMed (n=99)
- Activity (OpenAlex)
- Active — latest works 2026
- PublishLens list status
- Shown after sign-in
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Methodology signals (dated facts from their sources)
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Descriptive metadata from public sources (DOAJ, OpenAlex, PubMed) as of the capture date shown — contains no assessment or judgment.
Works in OpenAlex
3902
Last recorded publication year
2026
Reported by OpenAlex in 1 of 3 sources (CC0 flags, not verified indexing)DOAJSciELOOpenAlex Core
h-index
112
i10-index
2506
From OpenAlex open data (CC0).
Editorial & policy5
- Observed digital preservation (Keepers registry)— snapshot 2026-10-05
- CLOCKSSPortico
- Norwegian register (HK-dir)— 2026
- Level 1 — approved scholarly channel
- Open references deposited at Crossref
- 95%
- ORCID iDs in current deposits
- 82%
- Enrolled in Crossref Similarity Check
- ✓
- Deposits licence metadata at Crossref
- ✓
Identity & continuity2
- Source type
- journal
- NLM unique ID (PubMed)
- 9808008
Classification(no data)
No data available to the platform for this group
No platform data for: Classification — absence is not a judgment about the journal.
Subject areas
- Genetic Associations and Epidemiology
- Genetic Associations and Epidemiology
- Genetic Associations and Epidemiology
- Genomics and Rare Diseases
- Metabolism and Genetic Disorders
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Forensic and Genetic Research
Show all subjects (75)
- Genomic variations and chromosomal abnormalities
- Genomic variations and chromosomal abnormalities
- Hereditary Neurological Disorders
- Genomics and Rare Diseases
- Genomics and Rare Diseases
- Genetic diversity and population structure
- Genetics and Neurodevelopmental Disorders
- Genetics and Neurodevelopmental Disorders
- RNA modifications and cancer
- RNA modifications and cancer
- Mitochondrial Function and Pathology
- Mitochondrial Function and Pathology
- Metabolism and Genetic Disorders
- Metabolism and Genetic Disorders
- Genetic Mapping and Diversity in Plants and Animals
- Lysosomal Storage Disorders Research
- Forensic and Genetic Research
- Forensic and Genetic Research
- Glycogen Storage Diseases and Myoclonus
- Epigenetics and DNA Methylation
- Epigenetics and DNA Methylation
- Prenatal Screening and Diagnostics
- Prenatal Screening and Diagnostics
- Pharmacogenetics and Drug Metabolism
- RNA Research and Splicing
- Genetic Neurodegenerative Diseases
- RNA Research and Splicing
- RNA and protein synthesis mechanisms
- RNA and protein synthesis mechanisms
- Genetic factors in colorectal cancer
- Genetic Syndromes and Imprinting
- Genetic Syndromes and Imprinting
- Connective tissue disorders research
- RNA regulation and disease
- Genetic Neurodegenerative Diseases
- RNA regulation and disease
- Genetic Neurodegenerative Diseases
- Mitochondrial Function and Pathology
- Muscle Physiology and Disorders
- BRCA gene mutations in cancer
- Lysosomal Storage Disorders Research
- Lysosomal Storage Disorders Research
- BRCA gene mutations in cancer
- BRCA gene mutations in cancer
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Folate and B Vitamins Research
- Folate and B Vitamins Research
- Connective tissue disorders research
- Connective tissue disorders research
- Cancer-related molecular mechanisms research
- Cancer-related molecular mechanisms research
- Chromosomal and Genetic Variations
- Genetic diversity and population structure
- Genetic diversity and population structure
- Chromosomal and Genetic Variations
- Genetic and Kidney Cyst Diseases
- Congenital heart defects research
- Congenital heart defects research
- DNA Repair Mechanisms
- DNA Repair Mechanisms
- Prenatal Screening and Diagnostics
- Hearing, Cochlea, Tinnitus, Genetics
- Genetic Syndromes and Imprinting
- Hereditary Neurological Disorders
- Neurogenetic and Muscular Disorders Research
- Genetic and rare skin diseases.
- RNA Research and Splicing
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